510(k) K955651 ยท DQY Catheter, Percutaneous
MEDTRONIC SHERPA GUIDING CATHETER
| Applicant | Medtronics Interventional Vascular, Danvers MA, US |
| Decision | Substantially Equivalent, Jan 22, 1996 |
| Received | Dec 12, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K955651
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.